Triglycerides colorimetric assay kit

Manufactured by Elabscience

The Triglycerides colorimetric assay kit is a laboratory product designed to quantitatively determine the triglyceride concentration in a sample. The kit utilizes a colorimetric method to measure the absorbance of the reaction product, which is proportional to the triglyceride concentration in the sample.

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Lab products found in correlation

Microplate reader, by Thermo Fisher Scientific (2 mentions) Alkaline phosphatase activity assay kit, by Elabscience (1 mentions) Elisa kits for rat insulin, by Elabscience (1 mentions) Hdl c colorimetric assay kit, by Elabscience (1 mentions) Oil red, by Solarbio (1 mentions)

Close spelling variants of this product

Colorimetric assay kit Colorimetric assay

2 protocols using triglycerides colorimetric assay kit

Comprehensive Biochemical Assays for Metabolic Profiling

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Colorimetric assay kits for glucose (Cat # E-BC-K234, Elabscience Biotechnology
Inc.), alkaline phosphatase activity assay kit (Cat # E-BC-K091, Elabscience
Biotechnology Inc.), and alanine aminotransferase activity assay kit (Cat #
E-BC-K235, Elabscience Biotechnology Inc.); ELISA kits for rat insulin (Cat #
E-EL-R3034, Elabscience Biotechnology Inc.), rat IL-6 (Cat # E-EL-R0015,
Elabscience Biotechnology Inc.), and TNF alpha (Cat # E-EL-R0019, Elabscience
Biotechnology Inc.). Creatinine (Cr) colorimetric assay kit (Cat # E-BC-K188-M,
Elabscience Biotechnology Inc.), high-density lipoprotein cholesterol (HDL-C)
colorimetric assay kit (Cat # E-BC-K222-S, Elabscience Biotechnology Inc.), and
triglycerides colorimetric assay kit (Cat # E-BC-K261-M, Elabscience
Biotechnology Inc.). GLP-1 assay kit (Cat # E-EL-R3007, Elabscience
Biotechnology Inc.). Readings for ELISA kits were taken using Microplate ELISA
Reader (BIOBASE-EL 10A).

Javed A., Muzammal A., Akash M.S, & Rehman K. (2022). Biochemical Investigation of Therapeutic Potentials of Plant-Based Bioactive Compounds as Stimulators of Glucagon like peptide-1 Secretion. Dose-Response, 20(3), 15593258221114184.

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Adipogenic Differentiation and Muscular Fatty Infiltration

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Tissue slices or cultured cells were first fixed in 4% paraformaldehyde for 10 min, followed by oil red (Solarbio, cat#G1260) treatment for 10 min. Then samples were stained with hematoxylin for 5 min and mounted with 10% glycerol. For quantification analysis of lipid after adipogenic differentiation, the oil red was extracted by isopropanol for 5 min, and the value at 496 nm absorbance was detected by a microplate reader (Thermo Fisher Scientific).
Triglycerides colorimetric assay kit (Elabscience, cat#E-BC-K261-M) was employed to quantify the muscular fatty infiltration after tendon injury. Briefly, the muscle was first grounded with isopropanol (ACMEC, cat#I86620). Then tissue fragments were discarded by centrifugal machine at 10000 × g for 3 min. The supernatant was used to detect triglycerides by microplate reader at 510 nm absorbance.

Lin X., Wang P., Wang W., Zhou H., Zhu S., Feng S., Chen Y., Zhou H., Wang Q., Xin H., Shao X, & Wang J. (2023). Suppressed Akt/GSK-3β/β-catenin signaling contributes to excessive adipogenesis of fibro-adipogenic progenitors after rotator cuff tears. Cell Death Discovery, 9, 312.

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